Variant #0000795062 (NC_000003.11:g.100994537del, IMPG2(NM_016247.3):c.636del)

Individual ID 00380370
Chromosome 3
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100994537del
DNA change (hg38) -
Published as c.636delA
ISCN -
DB-ID IMPG2_000106 See all 2 reported entries
Variant remarks -
Reference PubMed: Bocquet-2013
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IMPG2 NM_016247.3 +/. 6 c.636del r.(?) p.(Glu213Argfs*18)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000381584 DNA PCR blood - IMPG2 1 LOVD